LivingGLP1
Descriptive only

Diabetic ketoacidosis

Type 1 diabetes

longest follow-upRecorded harmsDoses of a drug pooledHazard ratio (from event counts)
2
Randomized trials
3
Treatments
42
Participants
0
Events

In plain language

No network meta-analysis was fitted here. The protocol requires at least two trials forming a connected network; this outcome has 2 trials. The trial data below are shown as reported.

Network of trials

Each circle is a treatment; each line joins treatments that were randomized against each other in at least one trial.
LIRA_SCPLACEBOTIRZ_SC
Node area shows participants; line width shows trials comparing two treatments directly. Blue: GLP-1 receptor agonist containing treatments; grey: comparators. Hover over or tab to a node or line for details.

Comparability of the trials

Checked across designs (the set of treatments each trial compares) for eligibility, outcome definition and assessment, and the baseline factors above. Flags point to possible intransitivity; notes describe variation that is not tied to design.
  • FlagRisk of bias, funding: confounded with design: mixed 1, non_industry 1
  • FlagOutcome assessment, analysis set: confounded with design: randomized 1, safety 1
  • FlagOutcome assessment, definition: confounded with design: not stated 1, severe hypoglycemia, undefined 1
  • NoteOutcome assessment, time point: selected time points span 12 to 65 weeks
Comparability items per trial
Trialtime weeksanalysis setdefinitioninstrumentadjudicatedproportion methodintercurrent events (discontinuation)intercurrent events (rescue)blindingfundingstart yearEligibility
NCT0261765465randomizednot statednot statednot statednot statednot statednot stateddouble_blindmixed2015age 18 or older; T1D 5 years or longer; HbA1c 45 to 75 mmol/mol; fasting C-peptide above 1.5 pmol/L
S00300712safetysevere hypoglycemia, undefinednot statednot statednot statednot statednot stateddouble_blindnon_industry2024age 18 to 60; type 1 diabetes 2 years or more; BMI 30 or more

Trial data

What each trial contributes. Arm rows give the arm value with its standard error, or events over participants; contrast rows give the hazard ratio (from event counts) on the analysis scale (log) against the trial's first row. Flags mark converted, combined or approximated inputs.
Trial data entering this analysis
TrialArmTreatmentWeekDataValueSEEvents / NFlagsSource
NCT02617654A1PLACEBO65arm, events0 / 8R0012710:Results
NCT02617654A2LIRA_SC65arm, events0 / 10R0012710:Results
S003007A1TIRZ_SC12arm, events0 / 12R0014500:Results
S003007A2PLACEBO12arm, events0 / 12R0014500:Results

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